Zantac 150 Maximum Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Chattem, Inc.. The primary component is Ranitidine Hydrochloride.
| Product ID | 41167-0310_09ec7ce6-df1a-432f-b64a-afb1a7554a59 | 
| NDC | 41167-0310 | 
| Product Type | Human Otc Drug | 
| Proprietary Name | Zantac 150 Maximum Strength | 
| Generic Name | Ranitidine Hydrochloride | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA021698 | 
| Labeler Name | Chattem, Inc. | 
| Substance Name | RANITIDINE HYDROCHLORIDE | 
| Active Ingredient Strength | 150 mg/1 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2020-12-31 | 
| Marketing Start Date | 2018-11-11 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-10-12 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-08-17 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-04-03 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-08-17 | 
| Marketing Category | NDA | 
| Application Number | NDA021698 | 
| Product Type | HUMAN OTC DRUG | 
| Marketing Start Date | 2018-11-11 | 
| Ingredient | Strength | 
|---|---|
| RANITIDINE HYDROCHLORIDE | 150 mg/1 | 
| SPL SET ID: | 78380bf5-7ab6-42da-a02c-24644db778ff | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 21130-003 | Acid Reducer | Ranitidine Hydrochloride | 
| 46084-031 | APTIDINE | RANITIDINE HYDROCHLORIDE | 
| 0440-2300 | Ranitidine | Ranitidine Hydrochloride | 
| 11822-4727 | Ranitidine | Ranitidine Hydrochloride | 
| 11822-6051 | Ranitidine | Ranitidine Hydrochloride | 
| 11822-6052 | Ranitidine | Ranitidine Hydrochloride | 
| 11822-6107 | Ranitidine | Ranitidine Hydrochloride | 
| 37808-302 | Ranitidine | Ranitidine Hydrochloride | 
| 37808-303 | Ranitidine | Ranitidine Hydrochloride | 
| 41163-353 | Ranitidine | Ranitidine Hydrochloride | 
| 43353-952 | Ranitidine | Ranitidine Hydrochloride | 
| 49035-117 | Ranitidine | Ranitidine Hydrochloride | 
| 49035-353 | Ranitidine | Ranitidine Hydrochloride | 
| 50090-4353 | Ranitidine | Ranitidine Hydrochloride | 
| 0615-1354 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 0781-1883 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 0781-1884 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 0781-2855 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 0781-2865 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 15127-711 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 21695-337 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 21695-338 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 42291-735 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 42291-736 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 42291-766 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 42291-767 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 51079-879 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 51407-097 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 51407-098 | Ranitidine Hydrochloride | Ranitidine Hydrochloride | 
| 0173-0393 | ZANTAC | ranitidine hydrochloride | 
| 41167-0310 | Zantac 150 | Ranitidine Hydrochloride | 
| 41167-0320 | Zantac 150 | Ranitidine Hydrochloride | 
| 41167-0300 | Zantac 75 | Ranitidine Hydrochloride | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ZANTAC 150  78427712  3080635 Live/Registered | CHATTEM, INC. 2004-06-01 |